Importance of mobile genetic element immunity in numerically abundant Trichodesmium clades
Importance of mobile genetic element immunity in numerically abundant Trichodesmium clades
Date
2023-02-23
Authors
Webb, Eric A.
Held, Noelle A.
Zhao, Yiming
Graham, Elaina D.
Conover, Asa E.
Semones, Jake
Lee, Michael D.
Feng, Yuanyuan
Fu, Fei-Xue
Saito, Mak A.
Hutchins, David A.
Held, Noelle A.
Zhao, Yiming
Graham, Elaina D.
Conover, Asa E.
Semones, Jake
Lee, Michael D.
Feng, Yuanyuan
Fu, Fei-Xue
Saito, Mak A.
Hutchins, David A.
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DOI
10.1038/s43705-023-00214-y
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Abstract
The colony-forming cyanobacteria Trichodesmium spp. are considered one of the most important nitrogen-fixing genera in the warm, low nutrient ocean. Despite this central biogeochemical role, many questions about their evolution, physiology, and trophic interactions remain unanswered. To address these questions, we describe Trichodesmium pangenomic potential via significantly improved genomic assemblies from two isolates and 15 new >50% complete Trichodesmium metagenome-assembled genomes from hand-picked, Trichodesmium colonies spanning the Atlantic Ocean. Phylogenomics identified ~four Nfixing clades of Trichodesmium across the transect, with T. thiebautii dominating the colony-specific reads. Pangenomic analyses showed that all T. thiebautii MAGs are enriched in COG defense mechanisms and encode a vertically inherited Type III-B Clustered Regularly Interspaced Short Palindromic Repeats and associated protein-based immunity system (CRISPR-Cas). Surprisingly, this CRISPR-Cas system was absent in all T. erythraeum genomes, vertically inherited by T. thiebautii, and correlated with increased signatures of horizontal gene transfer. Additionally, the system was expressed in metaproteomic and transcriptomic datasets and CRISPR spacer sequences with 100% identical hits to field-assembled, putative phage genome fragments were identified. While the currently CO-limited T. erythraeum is expected to be a 'winner' of anthropogenic climate change, their genomic dearth of known phage resistance mechanisms, compared to T. thiebautii, could put this outcome in question. Thus, the clear demarcation of T. thiebautii maintaining CRISPR-Cas systems, while T. erythraeum does not, identifies Trichodesmium as an ecologically important CRISPR-Cas model system, and highlights the need for more research on phage-Trichodesmium interactions.
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© The Author(s), 2023. This article is distributed under the terms of the Creative Commons Attribution License. The definitive version was published in Webb, E. A., Held, N. A., Zhao, Y., Graham, E. D., Conover, A. E., Semones, J., Lee, M. D., Feng, Y., Fu, F.-X., Saito, M. A., & Hutchins, D. A. Importance of mobile genetic element immunity in numerically abundant Trichodesmium clades. ISME Communications, 3(1), (2023): 15, https://doi.org/10.1038/s43705-023-00214-y.
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Webb, E. A., Held, N. A., Zhao, Y., Graham, E. D., Conover, A. E., Semones, J., Lee, M. D., Feng, Y., Fu, F.-X., Saito, M. A., & Hutchins, D. A. (2023). Importance of mobile genetic element immunity in numerically abundant Trichodesmium clades. ISME Communications, 3(1), 15.